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iGluR

iGluR

The neurotransmitter glutamate activates the iGluR (ionotropic glutamate receptor), an ion channel that is ligand-gated. The central ion channel pore is formed by four large subunits of the integral membrane protein iGluR. All known glutamate receptor subunits, including the AMPA, kainate, NMDA, and  receptors, share a similar amino acid sequence.

The primary charge carriers during basal transmission are AMPA receptors, which allow an influx of sodium ions to depolarize the postsynaptic membrane. Magnesium ions block NMDA receptors, which only allow ion flux after a previous depolarization. They can now serve as coincidence detectors for synaptic plasticity because of this. NMDA receptors allow calcium to enter the body, which permanently changes how strongly synaptic transmission is carried out.
 

iGluR related products

Structure Cat No. Product Name CAS No. Product Description
(2R,3S)-Chlorpheg V70457 (2R,3S)-Chlorpheg 140924-23-8 (2R,3S)-Chlorpheg is a weak antagonist of L-homocysteine (L-HCA)-induced depolarization.
(R)-3C4HPG V70461 (R)-3C4HPG 13861-03-5 (R)-3C4HPG is an NMDA receptor blocker (antagonist).
(R)-Lanicemine ((R)-Lanicemine; (R)-AZD6765) V70475 (R)-Lanicemine ((R)-Lanicemine; (R)-AZD6765) 190581-71-6 (R)-Lanicemine ((R)-AZD6765) is the less active R-isomer of Lanicemine.
(R,S)-3,4-Dicarboxyphenylglycine ((R,S)-3,4-DCPG) V70433 (R,S)-3,4-Dicarboxyphenylglycine ((R,S)-3,4-DCPG) 176796-64-8 (R,S)-3,4-Dicarboxyphenylglycine ((RS)-3,4-DCPG) is an AMPA receptor antagonist.
(Rac)-Lanicemine ((Rac)-Lanicemine; (Rac)-AZD6765) V70395 (Rac)-Lanicemine ((Rac)-Lanicemine; (Rac)-AZD6765) 61890-25-3 (Rac)-Lanicemine ((Rac)-AZD6765) is the racemate of Lanicemine.
(Rac)-NMDAR antagonist 1 V70413 (Rac)-NMDAR antagonist 1 2435557-99-4 (Rac)-NMDAR antagonist 1 is the racemate of NMDAR antagonist 1.
(RS)-AMPA hydrobromide ((±)-AMPA hydrobromide) V70485 (RS)-AMPA hydrobromide ((±)-AMPA hydrobromide) 171259-81-7 (RS)-AMPA ((±)-AMPA) HBr is a glutamate analogue and a potent and specific agonist of the excitatory neurotransmitter L-glutamic acid.
(RS)-AMPA monohydrate ((±)-AMPA monohydrate) V70392 (RS)-AMPA monohydrate ((±)-AMPA monohydrate) 76463-67-7 (RS)-AMPA ((±)-AMPA) monohydrate is a glutamate analogue and a potent and specific agonist of the excitatory neurotransmitter L-glutamic acid.
(RS)-CPP ((±)-CPP) V70481 (RS)-CPP ((±)-CPP) 100828-16-8 (RS)-CPP ((±)-CPP) is a potent and specific NMDA antagonist.
(S)-(-)-HA 966 ((-)-HA 966) V70428 (S)-(-)-HA 966 ((-)-HA 966) 111821-58-0 (S)-(-)-HA 966 ((-)-HA 966) is a bioactive molecule similar to γ-hydroxybutyrate and a weakly active NMDA receptor antagonist.
(S)-AMPA (L-AMPA) V70411 (S)-AMPA (L-AMPA) 83643-88-3 (S)-AMPA (L-AMPA) is the active S-enantiomer of AMPA and is a potent and specific AMPA receptor agonist (activator).
1-Aminocyclobutanecarboxylic acid V70419 1-Aminocyclobutanecarboxylic acid 22264-50-2 1-Aminocyclobutanecarboxylic acid is a partial NMDA receptor agonist (activator) acting on the NR1 glycine site.
1-BCP V30846 1-BCP 34023-62-6 1-BCP (Piperonylic acid piperidide) is a centrally active molecule that regulates the gated current of AMPA receptors.
4′-Demethylnobiletin V69121 4′-Demethylnobiletin 34810-62-3 4′-Demethylnobiletin is a biobioactive metabolite that activates the PKA/ERK/CREB signaling pathway, enhances CRE-mediated transcription in hippocampal neurons, and reverses memory impairment associated with NMDA receptor antagonism by stimulating ERK signaling.
5,7-Dichlorokynurenic acid sodium (5,7-DCKA sodium) V85176 5,7-Dichlorokynurenic acid sodium (5,7-DCKA sodium) 1184986-70-6
5-Iodowillardiine V85165 5-Iodowillardiine 140187-25-3
6-Hydroxykynurenic acid (6-HKA) V70389 6-Hydroxykynurenic acid (6-HKA) 3778-29-8 6-Hydroxykynurenic acid (6-HKA) is an analogue of kynurenic acid (KYNA) and can be extracted from Ginkgo leaves.
AChE-IN-53 V84793 AChE-IN-53 2807436-94-6
Alaproclate hydrochloride (GEA 654 hydrochloride; A03 hydrochloride) V69998 Alaproclate hydrochloride (GEA 654 hydrochloride; A03 hydrochloride) 60719-83-7 Alaproclate (GEA 654) HCl is a selective, orally bioactive serotonin reuptake inhibitor (SSRI).
AMPA receptor modulator-2 V70425 AMPA receptor modulator-2 2034181-36-5 AMPA receptor modulator-2 (Example 134) is a modulator of AMPA receptors, with pIC50 of 10.1 for TARPγ2-dependent AMPA receptors.
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